A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv451355



Internal ID18621794
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:159205837..159332665hg38UCSC Ensembl
Innerchr7:158998526..159125355hg19UCSC Ensembl
Innerchr7:158691287..158818116hg18UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg38126829
hg19126830
hg18126830
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv428192
Supporting Variants
SamplesNA19189
Known Genes
MethodBAC aCGH
AnalysisCopy number variable segments were automatically detected using the CNVfinder algorithm (Fiegler et al. 2006).
PlatformSanger H. sapiens Whole Genome Tile Path 28.7k v3
Comments
ReferencePerry_et_al_2008b
Pubmed ID18775914
Accession Number(s)nssv451355
Frequency
Sample Size62
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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